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1. 2 Amino 2 Deoxyglucose
2. 2-amino-2-deoxyglucose
3. Dona
4. Dona S
5. Glucosamine
6. Hespercorbin
7. Sulfate, Glucosamine
8. Xicil
1. D-glucosamine Sulfate
2. 29031-19-4
3. (2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanal Sulfate
4. 33508-19-9
5. Glucosamine Sulphate
6. Dona
7. 2-amino-2-deoxy-d-glucose Sulfate (salt)
8. Gevolox
9. Arthro
10. Glucosaminsulfat
11. Sulfato De Glucosamina
12. Mfcd00135940
13. Einecs 249-379-6
14. Glucosamine Sulfate 2kcl
15. D-glucosamine Sulfate Salt
16. D-glucose, 2-amino-2-deoxy-, Sulfate (salt)
17. Glucosamine Sulfate Na Salt
18. Schembl22031
19. Glucosamine Sulfate Dc 95%
20. Dtxsid30944241
21. Hy-n0487
22. S3850
23. Ccg-267216
24. As-15566
25. Cs-0009005
26. Sulfuric Acid--2-amino-2-deoxyhexose (1/1)
27. A875270
28. W-107012
29. (2s,3s,5s)-3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol
30. 216447-61-9
| Molecular Weight | 277.25 g/mol |
|---|---|
| Molecular Formula | C6H15NO9S |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 5 |
| Exact Mass | 277.04675223 g/mol |
| Monoisotopic Mass | 277.04675223 g/mol |
| Topological Polar Surface Area | 207 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 223 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Glucosamine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Glucosamine manufacturer or Glucosamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glucosamine manufacturer or Glucosamine supplier.
PharmaCompass also assists you with knowing the Glucosamine API Price utilized in the formulation of products. Glucosamine API Price is not always fixed or binding as the Glucosamine Price is obtained through a variety of data sources. The Glucosamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hespercorbin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hespercorbin, including repackagers and relabelers. The FDA regulates Hespercorbin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hespercorbin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Hespercorbin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hespercorbin supplier is an individual or a company that provides Hespercorbin active pharmaceutical ingredient (API) or Hespercorbin finished formulations upon request. The Hespercorbin suppliers may include Hespercorbin API manufacturers, exporters, distributors and traders.
click here to find a list of Hespercorbin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hespercorbin DMF (Drug Master File) is a document detailing the whole manufacturing process of Hespercorbin active pharmaceutical ingredient (API) in detail. Different forms of Hespercorbin DMFs exist exist since differing nations have different regulations, such as Hespercorbin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hespercorbin DMF submitted to regulatory agencies in the US is known as a USDMF. Hespercorbin USDMF includes data on Hespercorbin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hespercorbin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hespercorbin suppliers with USDMF on PharmaCompass.
Hespercorbin Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Hespercorbin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Hespercorbin GMP manufacturer or Hespercorbin GMP API supplier for your needs.
A Hespercorbin CoA (Certificate of Analysis) is a formal document that attests to Hespercorbin's compliance with Hespercorbin specifications and serves as a tool for batch-level quality control.
Hespercorbin CoA mostly includes findings from lab analyses of a specific batch. For each Hespercorbin CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Hespercorbin may be tested according to a variety of international standards, such as European Pharmacopoeia (Hespercorbin EP), Hespercorbin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hespercorbin USP).
